Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Biochemical characterization of sporadic/familial hemiplegic migraine mutations.

Biochimica et biophysica acta - 1 Jul 2014

Weigand Karl M, Swarts Herman G P, Russel Frans G M, Koenderink Jan B

Abstract excerpt

Sporadic hemiplegic migraine type 2 (SHM2) and familial hemiplegic migraine type 2 (FHM2) are rare forms of hemiplegic migraine caused by mutations in the Na(+),K(+)-ATPase α2 gene. Today, more than 70 different mutations have been linked to SHM2/FHM2, randomly dispersed over the gene. For many o...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cell Membrane
Share to Hydrogen Bonding
Share to Migraine with Aura

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Models, Molecular

Share to Ouabain

Share to Sf9 Cells

Share to Sodium-Potassium-Exchanging ATPase

Share to Spodoptera

Source

Identifiers

PMID: 24704353
DOI: 10.1016/j.bbamem.2014.03.022

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24704353-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Biochemical characterization of sporadic/familial hemiplegic migraine mutations.PMID 24704353Read ↗

Diverse functional consequences of mutations in the Na+/K+-ATPase alpha2-subunit causing familial hemiplegic migraine type 2.Semantic proximity Read ↗

Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.Semantic proximity Read ↗

Functional effects of Na+,K+-ATPase gene mutations linked to familial hemiplegic migraine.Semantic proximity Read ↗

Na,K-ATPase mutations in familial hemiplegic migraine lead to functional inactivation.Semantic proximity Read ↗

Alterations in the alpha2 isoform of Na,K-ATPase associated with familial hemiplegic migraine type 2.Semantic proximity Read ↗

Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models.Semantic proximity Read ↗

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.Semantic proximity Read ↗

Two novel functional mutations in the Na+,K+-ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes.Semantic proximity Read ↗

Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.Semantic proximity Read ↗

Functional characterization of a novel C-terminal <i>ATP1A2</i> mutation causing hemiplegic migraine and epilepsySemantic proximity Read ↗

Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity.Semantic proximity Read ↗

Familial hemiplegic migraine.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.